Reaktion #1483844

ord-a7c7d16afd44470ba7763ed202991bbe

Lösungsmittel

Reaktionsbedingungen

Temperatur
100°CELSIUS
Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    Extraktionfollowed by extraction with ethyl acetate
  2. 2
    WaschenThe organic layer was washed with saturated brine
  3. 3
    Trocknendried over anhydrous magnesium sulfate
  4. 4
    Sonstigethe solvent was evaporated under reduced pressure
  5. 5
    SonstigeThe obtained residue was purified by silica gel column chromatography (chloroform/methanol)

Vorschrift

To a mixture of 3 g of methyl 4-fluoro-2-methoxy-5-nitrobenzoate, 1.99 g of 2-(tetrahydro-2H-pyran-4-yl)-1H-imidazole, and 15 mL of N-ethylpyrrolidone was added 3.6 g of potassium carbonate, followed by stirring at 100° C. for 3 hours. To the reaction mixture were added water and ethyl acetate, followed by extraction with ethyl acetate. The organic layer was washed with saturated brine and then dried over anhydrous magnesium sulfate, and the solvent was evaporated under reduced pressure. The obtained residue was purified by silica gel column chromatography (chloroform/methanol) to obtain 4.12 g of methyl 2-methoxy-5-nitro-4-[2-(tetrahydro-2H-pyran-4-yl)-1H-imidazol-1-yl]-benzoate.

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US08901126B2uspto-grants-2014_12